Linked Data
dbSNP Id:
rs1569484242
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8877T>C , J01415.2:m.8877T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.351T>C | ENSP00000354632.2:p.Phe117= |